The character graphics were created with a special graphics machine ("Character Generator Computer Aided Design") that generated a collection of all the graphical shapes used in the game.
In combination with five campaigns of ribosome display selection we generated a collection of 35 PSP94-binding clones called PAB binders, representing 29 unique sequence variants (Fig. 1A).
To determine which of these proteins might promote PB dispersion, we generated a collection of effector gene mutants and screened for their effect on PB integrity.
Therefore, to address this question, we generated a collection of anti BAFF-R mAbs some of which blocked and others failed to block BAFF binding.
We next generated a collection of entry clones for a set of ORFs of interest including markers expected to mark specific cell compartments including the nucleus, plasma membrane, basolateral membranes, whole microtubule network and centrosomes (Figure 2B).
To determine which parts of DNMT1 are required for cellular methyltransferase activity, we generated a collection of cDNAs expressing DNMT1 mutants that differ from each other in the sequence of a stretch of amino acids (Table 1).
We generated a collection of 118 constructs that contained the sequences of the 56 HCMV ORFs, including those coding for exons 1 and 2 of UL89, the amino and carboxyl domains of UL48, and exons 1 and 2 of UL112 (Figure 1, Supporting Information Table S2).
generated a collection of chicken neocentromeres in DT40 cells.
We generated a collection of ∼300,000 micrographs, comprising more than 20 million cells and ∼9 billion quantitative measurements.
We have generated a collection of 71 EMS-induced mutants that affect oocyte determination, polarization, or localization.
In the present study we have generated a collection of EST sequences from tissues of European seabass infected with V. anguillarum and Nodavirus.
